Markesbery W R, Lovell M A
Sanders-Brown Center on Aging, Department of Pathology, University of Kentucky, Lexington 40536-0230, USA.
Neurobiol Aging. 1998 Jan-Feb;19(1):33-6. doi: 10.1016/s0197-4580(98)00009-8.
Recent studies have implicated increased oxidative stress in the pathogenesis of Alzheimer's disease (AD). Increased lipid peroxidation and decreased polyunsaturated fatty acid levels have been described in the brain in AD. Four-hydroxynonenal (HNE), an aldehyde product of lipid peroxidation, has been demonstrated to be a neurotoxin in tissue culture and in vivo studies and is elevated in ventricular fluid in AD. We report here an increase in mean free HNE in multiple brain regions in AD compared with age-matched control subjects. These increases reached statistical significance in the amygdala and hippocampus and parahippocampal gyrus, regions showing the most pronounced histopathological alterations in AD. This study, in conjunction with cell culture studies, suggests that HNE may be an important substance in the pathogenesis of neuron degeneration in AD.
最近的研究表明,氧化应激增加与阿尔茨海默病(AD)的发病机制有关。AD患者大脑中脂质过氧化增加,多不饱和脂肪酸水平降低。脂质过氧化的醛产物4-羟基壬烯醛(HNE)在组织培养和体内研究中已被证明是一种神经毒素,且在AD患者的脑室液中升高。我们在此报告,与年龄匹配的对照受试者相比,AD患者多个脑区的游离HNE平均水平升高。这些升高在杏仁核、海马体和海马旁回达到统计学显著水平,这些区域在AD中显示出最明显的组织病理学改变。这项研究与细胞培养研究一起表明,HNE可能是AD中神经元变性发病机制中的一种重要物质。